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Stefan A Tschanz

Explore the profile of Stefan A Tschanz including associated specialties, affiliations and a list of published articles. Areas
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Articles 35
Citations 527
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Recent Articles
1.
Savas S, Tschanz S, Latzin P, Casaulta C, Muller L
Klin Padiatr . 2025 Feb; PMID: 39984160
No abstract available.
2.
Schierz A, Rossler G, Schneider J, Tschanz S, Werlein C, Jonigk D, et al.
Histochem Cell Biol . 2024 Nov; 163(1):7. PMID: 39557665
Alveolar epithelial type I (AE1) cells with their wide spatial expansion form approximately 95% of the outer surface area of the air-blood barrier inside the lung. Serial block-face scanning electron...
3.
Rossler G, Labode J, Schipke J, Tschanz S, Muhlfeld C
Pediatr Res . 2024 Sep; PMID: 39313553
Background: A comprehensive understanding of vascular development in the human lung is still missing. Methods: Therefore, samples of infant (n = 5, 26 days to 18 months postnatally) and adult...
4.
Schneiter M, Tschanz S, Escher A, Muller L, Frenz M
Comput Methods Programs Biomed . 2023 Aug; 241:107744. PMID: 37598471
Background And Objective: Primary ciliary dyskinesia (PCD) is a rare genetic disorder causing a defective ciliary structure, which predominantly leads to an impaired mucociliary clearance and associated airway disease. As...
5.
Escher A, Kieninger E, Groof S, Savas S, Schneiter M, Tschanz S, et al.
J Aerosol Med Pulm Drug Deliv . 2023 May; 36(4):171-180. PMID: 37196208
Inhalation of hypertonic saline (HS) is standard of care in patients with cystic fibrosis (CF). However, it is unclear if adding salbutamol has-besides bronchodilation-further benefits, for example, on the mucociliary...
6.
Fraenkl S, Simon Q, Yucel Y, Gupta N, Wittwer V, Frueh B, et al.
BMJ Open Ophthalmol . 2022 Sep; 7(1). PMID: 36161839
Objective: One of the most important risk factors for developing a glaucomatous optic neuropathy is elevated intraocular pressure. Moreover, mechanisms such as altered perfusion have been postulated to injure the...
7.
Haberthur D, Yao E, Barre S, Cremona T, Tschanz S, Schittny J
PLoS One . 2021 Nov; 16(11):e0257349. PMID: 34748555
Pulmonary acini represent the functional gas-exchanging units of the lung. Due to technical limitations, individual acini cannot be identified on microscopic lung sections. To overcome these limitations, we imaged the...
8.
Nussbaumer M, Kieninger E, Tschanz S, Savas S, Casaulta C, Goutaki M, et al.
ERJ Open Res . 2021 Nov; 7(4). PMID: 34729370
Background: Diagnosis of primary ciliary dyskinesia (PCD) is challenging since there is no gold standard test. The European Respiratory (ERS) and American Thoracic (ATS) Societies developed evidence-based diagnostic guidelines with...
9.
Muller L, Savas S, Tschanz S, Stokes A, Escher A, Nussbaumer M, et al.
Diagnostics (Basel) . 2021 Sep; 11(9). PMID: 34573882
Primary ciliary dyskinesia (PCD) is a rare genetic disease characterized by dyskinetic cilia. Respiratory symptoms usually start at birth. The lack of diagnostic gold standard tests is challenging, as PCD...
10.
Schneiter M, Halm S, Odriozola A, Mogel H, Ricka J, Stoffel M, et al.
J Struct Biol . 2020 Dec; 213(1):107680. PMID: 33359072
The tracheobronchial tree is lined by a mucociliary epithelium containing millions of multiciliated cells. Their integrated oscillatory activity continuously propels an overlying pollution-protecting mucus layer in cranial direction, leading to...